# Annotation for the copy number analysis of deep sequencing cancer data with seqCNA

## Documentation for package ‘seqCNA.annot’ version 0.99.1

- DESCRIPTION file.

## Help Pages

seqCNA.annot-package | Annotation for the copy number analysis of deep sequencing cancer data with seqCNA
hg18 | A table with GC content, mappability and presence of common CNVs for the hg18 human genome build.
hg18_len | A table with information on chromosome lengths for the hg18 human genome build.
hg19 | A table with GC content, mappability and presence of common CNVs for the hg19 human genome build.
hg19_len | A table with information on chromosome lengths for the hg19 human genome build.
seqCNA.annot | Annotation for the copy number analysis of deep sequencing cancer data with seqCNA
supported.builds | Names of the genome builds for which the package contains annotation.